A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234689



Internal ID20801729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:45651697..45659372hg38UCSC Ensembl
chr6:45619434..45627109hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg387676
hg197676
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6414333
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234689
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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